Abstract

The development of n -type conjugated polymers (CPs) forming an acceptor–acceptor (A–A)-type structure are quite challenging due to the synthetic limitation of imposing a functional group on the electron deficient aromatic structure. The diketopyrrolopyrroles (DPP) structure exhibits n -type characteristics; however, the extended π-structure enables stannylation at the terminal position. The stannylated DPP is beneficial for making n -type CPs, but its use in the development of n -type CPs and their application in n -type organic thin-film transistors and organic thermoelectric devices have been not extensively studied. In the present study, we synthesized the A–A-type conjugated polymer, poly [((2,5-bis(2-ethylhexyl)-3,6-di(thiophen-2-yl)-2,5-dihydropyrrolo [3,4- c ]pyrrole-1,4-dione)-5,5′-diyl)- alt -((2,7-bis(2-ethylhexyl)benzo [lmn] [3,8]phenanthroline-1,3,6,8(2 H ,7 H )-tetraone)-4,9-diyl))] (PDPP-NDI), by Stille coupling of distannylated DPP and dibrominated naphthalene diimide (NDI). The alternating copolymerization of DPP and NDI moieties led to a low-lying LUMO energy level of −4.4 eV, suitable for electron transport. The n -type organic thin-film transistors were fabricated with PDPP–NDI, and a substantial average electron mobility of 3.78 × 10 −2 cm 2 V −1 s −1 was obtained after thermal annealing. The n -type organic thermoelectric devices were developed via n -doping, and PDPP–NDI exhibited n -type thermoelectric properties, with an average power factor of 1.82 × 10 −3 μW m −1 K −2 . • An acceptor–acceptor-structured n -type alternating copolymer, PDPP–NDI, was developed. • A small bandgap of 1.03 eV and deep LUMO energy level of −4.4 eV were achieved. • The n -type characteristics of PDPP–NDI were successfully utilized in n -type OTFTs and OTE devices. • The device characteristics of both OTFT and OTE devices were fully studied and discussed.

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